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A clinical trial to study two Airway Equipments I-Gel and Laryngeal Tube Suction for Anesthetised patients

Comparison of I-Gel and Laryngeal Tube Suction during controlled ventilation

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2010/091/002993
Enrollment
60
Registered
2010-12-01
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: null- Study is conducted on patients undergoing elective surgery under General anesthesia.

Interventions

Intervention1: Usage of I-gel as airway equipment: Routine anesthetic drugs and agents used Control Intervention1: Airway equipment I-Gel or Laryngeal tube suction: Routine drugs will be used as for a

Sponsors

Institution
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA I , II Elective surgery under general anesthesia

Exclusion criteria

Exclusion criteria: Airway abnormalities Difficult Intubation Risk of aspiration Mouth opening less than 3cm

Design outcomes

Secondary

MeasureTime frame
Any risk of aspiration or throat problems following surgeryTimepoint: Post operative followup for 24 hrs—

Primary

MeasureTime frame
Efficacy of ventilation between cuffed and uncuffed supraglottic airway devicesTimepoint: Duration of surgery—

Countries

India

Contacts

Public ContactDrAshok sankar badhe
drkarunya@gmail.com08143769301

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026